dystrophy的例句大全

Facial emotion recognition in myotonic dystrophy type 1 correlates with CTG repeat expansion

1型强直性肌营养不良患者的面部表情识别与CTG的重复扩增相关

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Objective To carry out prenatal molecular diagnosis on 3 fetuses from different pedigrees with X-linked adrenoleukodystrophy ( ALD).

目的对3名来自不同家系的肾上腺脑白质营养不良（ALD）携带者所怀胎儿进行产前分子诊断。

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The molecular diagnosis for X linked adrenoleukodystrophy ( ALD) using mutational analysis at genomic DNA level is important.

在基因组DNA水平，应用基因突变分析的方法对肾上腺脑白质营养不良进行分子诊断十分重要。

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Cataract and myotonic dystrophy: the role of molecular diagnosis

强直性肌营养不良与白内障的分子诊断关系

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Clinical application of the molecular diagnostic technology for myotonic dystrophy

强直性肌营养不良的分子诊断技术的临床应用研究

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Not Brexit but Crispr gene-editing, a DNA-changing technology that can supposedly cure mice of liver disease and muscular dystrophy, render human cells resistant to HIV and create fungus-resistant wheat.

这里说的不是英国退欧，而是“成簇规律间隔短回文重复序列”（Crispr）基因编辑，一种据信能够治愈小鼠的肝病和肌营养不良，让人类细胞对艾滋病毒（HIV）产生抗性，培育出抗真菌小麦的DNA改造技术。

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Conclusions Clinically, Kennedy disease was easy to be misdiagnosed as polymyositis, limb-girdle muscular dystrophy, even Charcot-Marie-Tooth disease. AR gene testing is the most reliable diagnosing method.

结论临床上Kennedy病多被误诊为多发性肌炎、肢带型肌营养不良，甚至Charcot-Marie-Tooth病等，AR基因检测是诊断本病最可靠的方法。

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Lipid Metabolism of Endocrinopathy Lipodystrophy and ocular disease

内分泌疾病的脂代谢异常

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Prenatal molecular diagnosis of 3 Chinese X-linked adrenoleukodystrophy pedigrees

三个肾上腺脑白质营养不良家系的产前分子诊断

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Severe cardiac arrhythmias in young patients with myotonic dystrophy type 1

青年肌强直性营养不良Ⅰ型患者的严重心律失常

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Objective To explore the value of immunofluorescent technique for clinical diagnosing Duchenne muscular dystrophy ( DMD), Becker muscular dystrophy ( BMD) and Limb-girdle muscular dystrophy ( LGMD).

目的探讨免疫荧光检测对Duchenne型、Becker型和肢带型肌营养不良症（DMD、BMD和LG-MD）临床诊断的价值。

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Objective To explore the genotype-phenotype correlation of facioscapulohumeral muscular dystrophy ( FSHD) 1A gene.

目的探讨面肩肱型肌营养不良症（FSHD）1A的基因型与临床表型之间的相关关系。

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Progress in researches on the molecular genetics of facioscapulohumeral muscular dystrophy

面肩肱型肌营养不良症的分子遗传学研究进展

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Mechanism of translocation between chromosomes 4q and 10q in facioscapulohumeral muscular dystrophy

面肩肱型肌营养不良症患者染色体4q-10q相互易位机制的初步研究

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Gene diagnosis of facioscapulohumeral muscular dystrophy

面肩肱型肌营养不良症基因诊断

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Study on characteristics of gene structure and gene diagnosis of facioscapulohumeral muscular dystrophy using pulse field gel electrophoresis

应用脉冲场电泳技术研究面肩肱型肌营养不良症的基因突变特征及进行基因诊断

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Establishment of Pulsed Field Gel Electrophoresis System and Study on the Gene Structure of Facioscapulohumeral Muscular Dystrophy in Chinese Population

脉冲电场凝胶电泳技术体系的建立与中国人面肩肱型肌营养不良症的基因分析

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A clinical and ultrasounic examination was made on 120 sites of voluntary muscle from 29 cases with neuromuscular diseases, including varied muscular dystrophy, polymyositis, diversified neuro-genic myopathy and DMD possible carrier.

对29例神经肌肉疾病（包括多种肌营养不良，多发性肌炎，多种神经原性肌肉病变与DMD可能递体）的120处随意肌进行了临床与超声检查。

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Results The results showed Duchenne muscular dystrophy in 15 cases, congenital muscular dystrophy in 1 case and congenital myopathy ( sarcotubular myopathy) in 1 case.

结果活检病理诊断假性肥大性肌营养不良15例，先天性肌营养不良1例，先天性肌病（肌质管病）1例。

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Gene Mutation Analysis of Duchenne Muscular Dystrophy and Tuberous Sclerosis Complex

杜氏肌营养不良症和结节性硬化症的基因突变分析

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